A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437431



Internal ID22495301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11629864..11631095hg38UCSC Ensembl
chr8:11487373..11488604hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437431
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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